Doppler ultrasound uses blood flow signals to evaluate arteries and veins. It can detect abnormalities in flow patterns caused by stenosis or occlusion. The key parameters measured include peak systolic velocity (PSV), end diastolic velocity (EDV), and ratios of PSV in different vessel segments. Proper Doppler technique optimizes settings for sample volume placement, angle correction, and velocity scales. Common carotid artery (CCA) and internal carotid artery (ICA) waveforms are analyzed and compared bilaterally to detect asymmetries indicating stenosis. Degree of stenosis can be estimated from increased PSV ratios at and above areas of narrowing. Ulcerated or heterogeneous plaques on ultrasound also suggest unstable lesions.
Sonographic evaluation of breast Dr. Muhammad Bin Zulfiqar
In this we will discuss role of high resolution Ultrasound in breast pathologies.
We will further discuss the role of Elastography in characterization of BIRADS.
Urethral strictures are more commonly seen in the anterior urethra. They are commonly seen secondary to gonococcal urethritis or trauma. The normal urethral lumen is 4mm or less in diameter and has small thin walls. A stricture appears as a segment of narrowed lumen with irregularity and thickening of the wall due to fibrosis and scarring.
Sonographic evaluation of breast Dr. Muhammad Bin Zulfiqar
In this we will discuss role of high resolution Ultrasound in breast pathologies.
We will further discuss the role of Elastography in characterization of BIRADS.
Urethral strictures are more commonly seen in the anterior urethra. They are commonly seen secondary to gonococcal urethritis or trauma. The normal urethral lumen is 4mm or less in diameter and has small thin walls. A stricture appears as a segment of narrowed lumen with irregularity and thickening of the wall due to fibrosis and scarring.
The upper and lower extremity arteries , easy to examine, becoz of good imaging window.
Doppler frequencies are typically more than 3 MHz.
Though real-time gray-scale sonography is useful for evaluating the presence of atherosclerotic plaque or confirming the presence of extravascular masses. Color flow Doppler sonographic imaging allows the clinician to survey the area of interest rapidly, determine if vascular structures are present, and if so, characterize their blood flow patterns
Renal doppler is the most challenging test to perform due to small size of renal vessels, depth and anatomical variation. Its is used for accurate demonstration of vascular anatomy. It requires knowledge of local anatomy, normal waveform physiology and image optimization
Muktapishti is a traditional Ayurvedic preparation made from Shoditha Mukta (Purified Pearl), is believed to help regulate thyroid function and reduce symptoms of hyperthyroidism due to its cooling and balancing properties. Clinical evidence on its efficacy remains limited, necessitating further research to validate its therapeutic benefits.
Adv. biopharm. APPLICATION OF PHARMACOKINETICS : TARGETED DRUG DELIVERY SYSTEMSAkankshaAshtankar
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micro teaching on communication m.sc nursing.pdfAnurag Sharma
Microteaching is a unique model of practice teaching. It is a viable instrument for the. desired change in the teaching behavior or the behavior potential which, in specified types of real. classroom situations, tends to facilitate the achievement of specified types of objectives.
Antimicrobial stewardship to prevent antimicrobial resistanceGovindRankawat1
India is among the nations with the highest burden of bacterial infections.
India is one of the largest consumers of antibiotics worldwide.
India carries one of the largest burdens of drug‑resistant pathogens worldwide.
Highest burden of multidrug‑resistant tuberculosis,
Alarmingly high resistance among Gram‑negative and Gram‑positive bacteria even to newer antimicrobials such as carbapenems.
NDM‑1 ( New Delhi Metallo Beta lactamase 1, an enzyme which inactivates majority of Beta lactam antibiotics including carbapenems) was reported in 2008
Basavarajeeyam is an important text for ayurvedic physician belonging to andhra pradehs. It is a popular compendium in various parts of our country as well as in andhra pradesh. The content of the text was presented in sanskrit and telugu language (Bilingual). One of the most famous book in ayurvedic pharmaceutics and therapeutics. This book contains 25 chapters called as prakaranas. Many rasaoushadis were explained, pioneer of dhatu druti, nadi pareeksha, mutra pareeksha etc. Belongs to the period of 15-16 century. New diseases like upadamsha, phiranga rogas are explained.
Ozempic: Preoperative Management of Patients on GLP-1 Receptor Agonists Saeid Safari
Preoperative Management of Patients on GLP-1 Receptor Agonists like Ozempic and Semiglutide
ASA GUIDELINE
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DISSERTATION on NEW DRUG DISCOVERY AND DEVELOPMENT STAGES OF DRUG DISCOVERYNEHA GUPTA
The process of drug discovery and development is a complex and multi-step endeavor aimed at bringing new pharmaceutical drugs to market. It begins with identifying and validating a biological target, such as a protein, gene, or RNA, that is associated with a disease. This step involves understanding the target's role in the disease and confirming that modulating it can have therapeutic effects. The next stage, hit identification, employs high-throughput screening (HTS) and other methods to find compounds that interact with the target. Computational techniques may also be used to identify potential hits from large compound libraries.
Following hit identification, the hits are optimized to improve their efficacy, selectivity, and pharmacokinetic properties, resulting in lead compounds. These leads undergo further refinement to enhance their potency, reduce toxicity, and improve drug-like characteristics, creating drug candidates suitable for preclinical testing. In the preclinical development phase, drug candidates are tested in vitro (in cell cultures) and in vivo (in animal models) to evaluate their safety, efficacy, pharmacokinetics, and pharmacodynamics. Toxicology studies are conducted to assess potential risks.
Before clinical trials can begin, an Investigational New Drug (IND) application must be submitted to regulatory authorities. This application includes data from preclinical studies and plans for clinical trials. Clinical development involves human trials in three phases: Phase I tests the drug's safety and dosage in a small group of healthy volunteers, Phase II assesses the drug's efficacy and side effects in a larger group of patients with the target disease, and Phase III confirms the drug's efficacy and monitors adverse reactions in a large population, often compared to existing treatments.
After successful clinical trials, a New Drug Application (NDA) is submitted to regulatory authorities for approval, including all data from preclinical and clinical studies, as well as proposed labeling and manufacturing information. Regulatory authorities then review the NDA to ensure the drug is safe, effective, and of high quality, potentially requiring additional studies. Finally, after a drug is approved and marketed, it undergoes post-marketing surveillance, which includes continuous monitoring for long-term safety and effectiveness, pharmacovigilance, and reporting of any adverse effects.
Title: Sense of Taste
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the structure and function of taste buds.
Describe the relationship between the taste threshold and taste index of common substances.
Explain the chemical basis and signal transduction of taste perception for each type of primary taste sensation.
Recognize different abnormalities of taste perception and their causes.
Key Topics:
Significance of Taste Sensation:
Differentiation between pleasant and harmful food
Influence on behavior
Selection of food based on metabolic needs
Receptors of Taste:
Taste buds on the tongue
Influence of sense of smell, texture of food, and pain stimulation (e.g., by pepper)
Primary and Secondary Taste Sensations:
Primary taste sensations: Sweet, Sour, Salty, Bitter, Umami
Chemical basis and signal transduction mechanisms for each taste
Taste Threshold and Index:
Taste threshold values for Sweet (sucrose), Salty (NaCl), Sour (HCl), and Bitter (Quinine)
Taste index relationship: Inversely proportional to taste threshold
Taste Blindness:
Inability to taste certain substances, particularly thiourea compounds
Example: Phenylthiocarbamide
Structure and Function of Taste Buds:
Composition: Epithelial cells, Sustentacular/Supporting cells, Taste cells, Basal cells
Features: Taste pores, Taste hairs/microvilli, and Taste nerve fibers
Location of Taste Buds:
Found in papillae of the tongue (Fungiform, Circumvallate, Foliate)
Also present on the palate, tonsillar pillars, epiglottis, and proximal esophagus
Mechanism of Taste Stimulation:
Interaction of taste substances with receptors on microvilli
Signal transduction pathways for Umami, Sweet, Bitter, Sour, and Salty tastes
Taste Sensitivity and Adaptation:
Decrease in sensitivity with age
Rapid adaptation of taste sensation
Role of Saliva in Taste:
Dissolution of tastants to reach receptors
Washing away the stimulus
Taste Preferences and Aversions:
Mechanisms behind taste preference and aversion
Influence of receptors and neural pathways
Impact of Sensory Nerve Damage:
Degeneration of taste buds if the sensory nerve fiber is cut
Abnormalities of Taste Detection:
Conditions: Ageusia, Hypogeusia, Dysgeusia (parageusia)
Causes: Nerve damage, neurological disorders, infections, poor oral hygiene, adverse drug effects, deficiencies, aging, tobacco use, altered neurotransmitter levels
Neurotransmitters and Taste Threshold:
Effects of serotonin (5-HT) and norepinephrine (NE) on taste sensitivity
Supertasters:
25% of the population with heightened sensitivity to taste, especially bitterness
Increased number of fungiform papillae
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5. Arterial –Triphasic ( dec early dias due to inc
peripheral resis.
Inc late dias due to re elasticity
-biphasic ( due to re elasticity)
Venous –monophasic (cardiac and respiratory
modulations).
9. Before stenosis- normal Distal to stenosis-parvus-tardus
At site of stenosis- incr velocity
spectral broadening (mosaicing)
10. In case of partial arterial stenosis
If the stenosis is < 50%, the speed is normal.
50% stenosis, velocity will be 1.5-2 time.
50-75% 2-4 time.
>75% >4 time..
11. Color steer box
It should be as small as and superficial as possible.
Change angle of insonation between 30-60 to get
less error.
If not sufficient– angulation of the probe.
12.
13.
14.
15.
16. Adjust system gain;
Amplification of signal to provide good quality
Decrease Doppler gain ---inadequate color saturation
(Doppler mopping)
Increase Doppler---noise
Adjust color velocity scale (range of velocities used)
If aliasing --- increase
If abscent flow---decrease
17.
18.
19. Sample volume
The sample site from which the data obtained.
Used for pulse wave, not for continous wave.
It should be
Narrow zone 1/3 -2/3 of blood vessel diameter.
To decrease spectral broadening
Central in position– to acquire highest speed of flow.
If peripheral –slow motion of blood and vessel wall motion
detected.
Angle correct
Trying virtual to be inside the vessel (parallel to the lumen,
never exceed 60 degree.)
20.
21.
22.
23.
24. Pulse repetition frequency:
Range of velocities used
Spectral Doppler scale;
Same as color gain
Wall filter; not commonly used
Filter motion of wall motion in case of peripheral volume sampling
Frame rate;
Try to be high
Number of refreshing the images/sec
NB; flow direction; above base line toward the probe.
Below base line – away from the probe.
25.
26.
27.
28.
29.
30.
31.
32. Adv;
Very sensitive to very sluggish flow
No aliasing
Angle independent
Useful in tortuous vessels
Disadv;
Don’t provide flow velocity.
Unidirectional.
33.
34. Aliasing
Inability of device to
detect high blood flow
in PWD
Solution
Incr PRF
Down ward base line
Broadening of spectral
window
Spectral window ;black
Area under the curve(it
should be open)
1- wide sample volume;
narrow sample volume
2- high Doppler gain;
decrease gain
Turbulent flow
Physiological and
pathological.
Color Doppler inaccuracy
Over or under saturation
Of color in blood vessel or
abnormal color pattern
Causes;
1-Inadequate Doppler gain
--Doppler mopping
2- incr Doppler gain
Noise
3-inadequate steering
4-Aliasing; incr PRF
35. Resistive index=S-D/S
Pulsatility index=S-D/Mean
S/D; D/S
Acceleration index-change in distance between beginning
Of systole to the peak of systole cm/s
Normal value >3.8cm/s
Acceleration time-length of time in sec from onset of systole to the
peak.
Normal value <0.07 sec.
36.
37.
38. Patient Position
supine or semi supine
head slightly hyper‐extended
rotated 45°away from the side being examined.
Higher‐frequency linear transducers (7 MHz)
39. Vessels should be imaged as completely as possible
•Caudal angulation of the transducer in the supra-
clavicular region and cephalic angulation at the
level of the mandible.
•Assessed both in gray scale and colour Doppler
settings.
40. Limitations
short muscular neck.
a high carotid bifurcation.
tortuous vessels.
calcified shadowing plaques.
41. Scan both in transverse and longitudinal plane.
•Starting from proximal most CCA, bulb, ECA and
ICA.
•Distal carotid ‐2 cm from the bulb.
•ICA or ECA ?
Large in caliber, posterior and lateral
low resistance wave form (not reliable)
no branches
no cluttering with temporal artery tapping.
42. Color Doppler Sampling Window
also known as the color box
The size is adjusted to include all regions of
interest.
Adjustment of the angle‐by changing the box
angles from left to center or right
angling the transducer to ensure that the
Doppler angle is less than 60°to the direction of
blood flow.
43.
44. If the Doppler angle is small or more than 60 degree
‐small error in the estimated velocity.
preferred angle of incidence is 45°±4.
The optimal position of the sample volume gate
in a normal artery is in the mid lumen parallel to the vessel
wall
in a diseased vessel, parallel to the direction of blood
flow
should not be placed on the sharp curves of a tortuous
artery ‐falsely high velocity reading.
Should not be placed too close to the vessel
wall‐spectral broadening.
45.
46. Spectral broadening results from turbulence in the
blood flow.
Spurious spectral broadening
a large Doppler angle
a sample volume gate located close to the vessel wall
a high Doppler gain setting
The size of the gate is normally ‐between 2 and 3 mm.
too small (1.5 mm) ‐the Doppler signal may be missed
too large >3.5 mm ‐spectral broadening
47. If set below the mean velocity of blood flow,
Aliasing throughout the vessel lumen.
set significantly higher than the mean velocity of
blood flow, aliasing may disappear resulting in a
missed stenosis
In a normal carotid US examination, the color
velocity scale should be set between 30 and 40
cm/sec(mean velocity).
48.
49. The color gain should be set so that color just
reaches the intimal surface of the vessel.
If the color gain setting is too low, trickle flow may
go undetected.
If a color gain setting is high, “bleeding” of the
color into the wall and surrounding tissues ‐limit
visualization of the plaque surface
50.
51. PDI may provide increased sensitivity to visualize
the continuity of blood flow in arterial stenosis
52. Defined as a localized protrusion from the
wall into the lumen with an area 50% greater
than the intima ‐media thickness of
neighboring sites.
low and high echogenic plaque.
heterogeneous or homogeneous.
regular (smooth) or irregular.
53. If more than 20% of the plaque echogenicity differed
from the echogenicity of the rest of the plaque by
two or more echogenicity grades –is heterogenous.
When height variations between 0.4 and 2 mm
along the contour of the lesion –is irregular
Ulcerated plaques‐recesses in the contour of the
lesion at least 2 mm in depth, with a well‐defined
back wall at the base showing flow.
54.
55. Heterogeneous plaques and ulcerated
plaques are unstable or friable.
Potential for embolicTIA and cerebrovascular
accidents.
58. Class I,homogeneous texture, uniformly hypoechoic
Class II,heterogeneous texture, predominantly
hypoechoic
Class III,heterogeneous texture, predominantly
hyperechoic
Class IV,homogeneous texture, uniformly
hyperechoic
ClassV,unclassified calcified plaques
59. After optimizing the setting ****
Measure the velocity –PSV and DV
Proximal and distal CCA
ICA and ECA
Vertebral artery
Wherever stenosis present –
at stenosis
proximal to and distal to stenosis
Compare bilateral carotid velocities –symmetric or asymmetric
60. combination of ICA and ECA patterns,
•intermediate amount of continuous forward diastolic flow
•a sharp systolic upstroke and thin spectral envelope
•flow below the baseline or filling in of the spectral window normally should not be
seen
61. a low‐resistance waveform pattern
•systolic peak should be sharp and the spectral envelope thin
•continuous forward diastolic flow
•the systolic peak may be slightly blunter than the systolic peak of the ECA
62. the systolic upstroke is sharp
•the spectral envelope is thin.
•reduced to no diastolic flow
•diastolic flow should be symmetrical bilaterally
•Transient reversal in early diastole (characteristic early diastolic notch ) ‐a normal finding
65. Either low or high PSVs.
abnormally high‐resistance waveform,
an abnormally low‐resistance
waveform.
66. A normal CCA PSV should be in the range of
approximately 60 –100 Cm/s
•IF less than this, examine opposite side
Symmetric Asymmetric
(near normal)
Low cardiac output
Evaluate further
A velocity difference of >20 cm/sec between the
right and left is abnormal.
67. Proximal stenosis (brachiocephalic)
Parvus ‐tardus waveform or normal pattern
but asymmetrical PSVs.
Distal stenosis (carotid bulb level)
High resistance wave form
69. High-resistance waveform in CCA
High‐grade ICA stenosis or occlusion
(externalization of the CCA)
Distal waveforms should be assessed (support the
diagnosis)
EXCEPTION IF
???
is bilateral and low PSVs indicates
Aortic stenosis
Severe cardiac failure
72. The ratio of the highest PSV at the CCA
stenosis divided by the PSV 2 cm proximal to
the stenosis should be calculated.
PSVcca at stenosis/PSVcca prox.
If the ratio is 2 or more and less than 2.99
‐stenosis of 50% or more.
If the ratio is 3 or more stenosis of 75% or
more.
74. Unusual finding in Case of CCA
occlusion .Reversal of flow in ECA
and low resistance and low PSVs in
ICA as it is fed by collaterals.
This is to maintain the ante grade
flow in ICA.
75.
76.
77. If the stenosis is unilateral, there is marked
asymmetry in the systolic contour of the
waveforms of the right and the left CCAs.
If the stenosis is central, such as with aortic
stenosis, the waveforms are affected
bilaterally.
78. Normal is ‐low resistance with high diastolic
pattern.
Most common site is ICA origin –plaque
extending from the bulb.
High resistance pattern in the ICA‐Stenosis
distally.
PSVs raises ‐Significant stenosis
84. So assess ICA
•In gray scale for amount of luminal narrowing
•Assess velocities in proper settings
•Should assess PSV, EDV and ratio of PSVs in ICA
and CCA
•Assessed proximally, mid and distally.
•If no color flow demonstrated in a tight stenotic
segment even in power Doppler confirm with
other modality
•Assess opposite ICA for compensatory flow
85. Confirm the ECA
Is there any reversal of flow
Is there any internalization
87. PULSUS BISFERIENCE
‘‘beat twice,’’
Characterized by two systolic peaks with an
interposed mid systolic retraction
Seen in
AR with or without concomitant AS
Hypertrophic obstructive cardiomyopathy
Occasionally, may be seen in healthy, athletic,
young individuals or in older patients.
91. water hammer pulse’’
In aortic regurgitation –reversed early diastolic
flow in both CCAs with elevation of PSV and a
sharp systolic upstroke
Depending on the severity, the reversal of flow
may be limited to early diastole with
normalization of forward flow in end Diastole
or may persist throughout diastole.
92.
93. DISSECTION
•Trauma ‐seat belt injury or repetitive trauma.
•Occasionally, spontaneous and isolated to the carotid
arteries in Marfan syndrome, Ehlers‐Danlos syndrome,
fibromuscular dysplasia, hypertension, or drug abuse
•Also ‐direct extension of an aortic dissection.
•Rare but, dissection of the ICA is the most common
cause of stroke in young patients.
•Most ICA dissections occur at the level of the carotid
bifurcation.
94. Wave pattern is extremely bizarre in configuration:
low PSV velocity with a highly irregular waveform
contour with many spikes or fluttering with reversed
or bidirectional of flow, such that it may be difficult to
distinguish systole from diastole
•an intramural hematoma, causing a long‐segment
tapering of the ICA without a break in the intima
•The residual lumen may be narrowed markedly,
creating a ‘‘string sign.’’
95. Thrombosis of the false lumen ‐mimic
stenosis
The waveform may be indistinguishable from
a stenosis except that typically it extends
over a much longer segment and often no
plaque is visualized.
96. The presence of early diastolic flow reversal
in the ipsilateral CCA
•reduced peak systolic and diastolic velocities
in the ipsilateral ICA
are non‐specific, but warrant a search for a
cause of increased peripheral vascular
resistance.